Primary Device ID | 08800053063845 |
NIH Device Record Key | 691c7161-3c2d-4530-a565-35bdbe72d77a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | M200 Series (Ceiling, Mobile) |
Version Model Number | M200 |
Company DUNS | 694721181 |
Company Name | DENTIS CO. ,LTD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |